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Chronic Inflammatory Demyelinating Polyneuropathy Associated With Tumor Necrosis Factor-Α Antagonists Publisher Pubmed



Alshekhlee A1 ; Basiri K1, 2 ; Miles JD1, 3 ; Ahmad SA1 ; Katirji B1
Authors
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Authors Affiliations
  1. 1. Neurological Institute, University Hospitals Case Medical Center, Case Western Reserve University, Cleveland, OH 44106-5040, 11100 Euclid Avenue, United States
  2. 2. Department of Neurology, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Marshall University, Huntington, WV, United States

Source: Muscle and Nerve Published:2010


Abstract

Biologic therapy with tumor necrosis factor (TNF)-α antagonists for rheumatoid arthritis has been well established. We describe two patients with rheumatoid arthritis who developed chronic inflammatory demyelinating polyneuropathy (CIDP) during their course of therapy with TNF-α antagonists. A 45-year-old woman and a 49-year-old man, both with a history of rheumatoid arthritis, were treated with etanercept and infliximab, respectively. Clinical signs of peripheral neuropathy developed 2 weeks and 12 months after the initiation of TNF-α antagonists. Electrodiagnostic studies at variable points during the disease course showed signs of acquired demyelination consistent with CIDP. Cerebrospinal fluid examination showed albuminocytologic dissociation (total protein concentration 118 mg/dl and 152 mg/dl, respectively). Both patients failed to improve after discontinuation of the offending agent, and they responded poorly to corticosteroids. However, there was clinical and electrophysiologic recovery after initiation of intravenous immunoglobulin (IVIg) therapy. CIDP may occur early or late during the treatment course with TNF-α antagonists. IVIg may reverse and stabilize the inflammatory process. © 2010 Wiley Periodicals, Inc.